Peutz-Jeghers Syndrome [Peutzův-Jeghersův syndrom]

topical
37
Terms

hamartomatózní polypóza
lentiginopolyposis digestiva
Peutzova-Jeghersova polypóza

 

Lentiginosis, Perioral
Periorificial Lentiginosis Syndrome
Peutz-Jegher's Syndrome
Peutz-Jeghers Polyposis
Polyposis, Hamartomatous Intestinal
Polyps-and-Spots Syndrome

Persistent link   https://www.medvik.cz/link/D010580
Definition

A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and mucocutaneous pigmentation with MELANIN spots of the lips, buccal MUCOSA, and digits.

DUI
D010580 MeSH Browser
CUI
M0016441
History note
65; was see under POLYPI (now POLYPS) 1963-64
Public note
65; was see under POLYPI (now POLYPS) 1963-64

Allowable subheadings

BL
blood 0
CF
cerebrospinal fluid 0
CI
chemically induced 0
CL
classification 0
CO
complications 4
DI
diagnosis 16
DG
diagnostic imaging 0
DH
diet therapy 0
DT
drug therapy 0
EC
economics 0
EM
embryology 0
EN
enzymology 0
EP
epidemiology 1
EH
ethnology 0
ET
etiology 5
GE
genetics 9
HI
history 0
IM
immunology 0
ME
metabolism 0
MI
microbiology 0
MO
mortality 0
NU
nursing 0
PS
parasitology 0
PA
pathology 4
PP
physiopathology 0
PC
prevention & control 2
PX
psychology 0
RT
radiotherapy 0
RH
rehabilitation 0
SU
surgery 6
TH
therapy 5
UR
urine 0
VE
veterinary 0
VI
virology 0

C Diseases
C04 Neoplasms 12 762
C04.700 Neoplastic Syndromes, Hereditary 143
C04.700.100 Adenomatous Polyposis Coli 92
C04.700.175 Basal Cell Nevus Syndrome 32
C04.700.212 Birt-Hogg-Dube Syndrome 8
C04.700.250 Colorectal Neoplasms, Hereditary Nonpolyposis 114
C04.700.305 Dysplastic Nevus Syndrome 17
C04.700.330 Exostoses, Multiple Hereditary 12
C04.700.435 Hamartoma Syndrome, Multiple 25
C04.700.517 Hereditary Breast and Ovarian Cancer Syndrome 53
C04.700.600 Li-Fraumeni Syndrome 39
C04.700.630 Multiple Endocrine Neoplasia 32
C04.700.631 Neurofibromatoses 28
C04.700.633 Peutz-Jeghers Syndrome 37
C04.700.700 Tuberous Sclerosis 141
C04.700.900 Wilms Tumor 112
C06 Digestive System Diseases 671
C06.405 Gastrointestinal Diseases 1 745
C06.405.469 Intestinal Diseases 756
C06.405.469.578 Intestinal Polyposis 27
C06.405.469.578.249 Adenomatous Polyposis Coli 92
C06.405.469.578.500 Cronkhite-Canada Syndrome
C06.405.469.578.750 Peutz-Jeghers Syndrome 37
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 213
C16.320.700 Neoplastic Syndromes, Hereditary 143
C16.320.700.100 Adenomatous Polyposis Coli 92
C16.320.700.175 Basal Cell Nevus Syndrome 32
C16.320.700.212 Birt-Hogg-Dube Syndrome 8
C16.320.700.250 Colorectal Neoplasms, Hereditary Nonpolyposis 114
C16.320.700.305 Dysplastic Nevus Syndrome 17
C16.320.700.330 Exostoses, Multiple Hereditary 12
C16.320.700.435 Hamartoma Syndrome, Multiple 25
C16.320.700.517 Hereditary Breast and Ovarian Cancer Syndrome 53
C16.320.700.600 Li-Fraumeni Syndrome 39
C16.320.700.630 Multiple Endocrine Neoplasia 32
C16.320.700.633 Neurofibromatoses 28
C16.320.700.667 Peutz-Jeghers Syndrome 37
C16.320.700.700 Tuberous Sclerosis 141
C16.320.700.900 Wilms Tumor 112
C17 Skin and Connective Tissue Diseases 32
C17.800 Skin Diseases 2 796
C17.800.621 Pigmentation Disorders 132
C17.800.621.430 Hyperpigmentation 65
C17.800.621.430.530 Melanosis 38
C17.800.621.430.530.550 Lentigo 16
C17.800.621.430.530.550.525 LEOPARD Syndrome 11
C17.800.621.430.530.550.625 Peutz-Jeghers Syndrome 37

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